HHSClass 3
Transcervical Contraceptive Tubal Occlusion Device
FDA adverse event reports and recall history for transcervical contraceptive tubal occlusion device (product code HHS), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 74,490
- Deaths
- 136
- Injuries
- 72,845
- Malfunctions
- 1,078
Reports per year
15312
80013
2,23714
5,96315
4,93216
11,84717
5,98318
15,08519
16,13520
3,72521
1,64022
3,63723
84824
75625
24126
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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